Effect of L-NAME, an inhibitor of nitric oxide synthesis, on plasma levels of IL-6, IL-8, TNFα and nitrite/nitrate in human septic shock

被引:31
作者
Avontuur, JAM [1 ]
Stam, TC
Jongen-Lavrencic, M
van Amsterdam, JGC
Eggermont, AMM
Bruining, HA
机构
[1] Univ Rotterdam Hosp, Dept Surg, Rotterdam, Netherlands
[2] Netherlands Red Cross Blood Transfus Serv, Dept Autoimmune Dis, Cent Lab, Amsterdam, Netherlands
[3] Expt & Clin Immunol Lab, Amsterdam, Netherlands
[4] Natl Inst Publ Hlth & Environm, Dept Pharmacol, Bilthoven, Netherlands
关键词
sepsis; nitric oxide; nitric oxide synthase inhibition; L-NAME; cytokines;
D O I
10.1007/s001340050643
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objectives: We tested the effects of N-G-nitro-L-arginine methyl ester (L-NAME), an inhibitor of nitric oxide (NO) synthesis, on plasma levels of interleukin (IL) IL-6, IL-8, tumor necrosis factor-alpha (TNF alpha) and nitrite/nitrate (NO2-/ NO3-) in patients with severe septic shock. Design: Prospective clinical study. Setting: Surgical intensive care unit at a university hospital. Patients: 11 consecutive patients with severe septic shock. Interventions: Standard hemodynamic measurements were made and blood samples taken at intervals before, during, and after a 12-h infusion of L-NAME 1 mg.kg(-1).h(-1) for determination of plasma IL-6, IL-8, TNF alpha and NO2-/NO3- concentration. Measurements and results: Patients with sepsis had increased plasma levels of IL-6, IL-8, TNF alpha and NO2-/NO3- (p<0.05), Plasma levels of IL-6. IL-8: and NO2-/NO3- were negatively correlated with systemic vascular resistance (r = -0.62, r = -0.65, and r = -0.78, respectively, all p < 0.05). Continuous infusion of L-NAME increased mean arterial pressure and systemic vascular resistance, with a concomitant reduction in cardiac output (all p < 0.01). No significant changes were seen in levels of plasma IL-6, IL-8, and NO2-/NO3- during the 24-h observation period. Plasma levels of TNF alpha were significantly reduced during L-NAME infusion compared to baseline (p < 0.05), Conclusions: NO plays a role in the cardiovascular derangements of human septic shock. Inhibition of NO synthesis with L-NAME does not promote excessive cytokine release in patients with severe sepsis.
引用
收藏
页码:673 / 679
页数:7
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